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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798901Generated: October 31, 2026

1,4-Dioxane hydrochloride → HCID 178503322, compound

https://huagongshe.com/reaction/1798901

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 178503325HCID 178503325—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178503322HCID 178503322—

Reaction Steps

4 M dioxane-HCl (300 mL) was added to crude 7-(methylthio)-5-phenyl-1,3,4,5-tetrahydro-1,2,5,6,8-pentaazaacenaphthylene-3-carboxylic acid (20 g) and the mixture was refluxed for 16 h. Upon completion of reaction after 16 h (monitored by LCMS), dioxane was removed under reduced pressure and saturated NaHCO3 solution (200 mL) was added. The reaction mixture was then extracted with dichloromethane (150 mL×3). The combined organic layer was dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by silica gel column chromatography (using 0-10% tetrahydrofuran in dichloromethane) to provide 7-(methylthio)-5-phenyl-1,3,4,5-tetrahydro-1,2,5,6,8-pentaazaacenaphthylene as a white solid after recrystalized from ethyl acetate (4.2 g, 26.7% yield for three steps). 1H NMR (DMSO-d6, 400 MHz) δ 13.02 (s, 1H); 7.53-7.23 (m, 5H); 4.19 (t, J=6.4 Hz, 2H); 3.21 (t, J=6.4 Hz, 2H); 2.42 (s, 3H). LCMS [M+H]: 284 HPLC: 98.28% (254 nm)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343983B2
Source datasetuspto-grants-2013_01
ORD IDord-e0fec1682bde49c2a4437835df980f85
Source noteuspto-grants-2013_01